BEUDAMED
    11 results · 32ms · Sources: EU EUDAMED, US FDA

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    MICROLIFE WRIST WATCH BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MAGNUM INSTRUMENTATION

    FDA UDI
    Biomet Uk Ltd·05019279440436·

    M2a-Magnum™

    FDA UDI
    Biomet Orthopedics, LLC·00887868474378·

    PHILIPS AVALON FETAL/MATERNAL MONITORS FM20, FM30, FM40 AND FM50

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    DSS STABILIZATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MENTOR SILTEX ROUND MODERATE PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·May 25, 2022

    MENTOR SILTEX ROUND MODERATE PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·May 26, 2022

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·June 3, 2013

    ENDEAVOR SPRINT RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·June 21, 2011

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 3, 2008

    3.0 mm Reaming Rod/950 mm w/straight Ball Tip, Sterile

    FDA Enforcement
    Class II ·Terminated·Synthes (USA) Products LLC·November 30, 2016